Journal of Infectious Diseases & Therapy
Open Access

COVID-19: Coronavirus Disease-2019; CAPA: COVID-19 Associated Pulmonary Aspergillosis; IL-6: Interleukin-6; IPA: Invasive Pulmonary Aspergillosis; ICU: Intensive Care Unit; LOS: Length of Stay; IMV: Invasive Mechanical Ventilation; SARS-CoV-2: Severe Acute Respiratory Syndrome Coronavirus 2 IAPA: Influenza- Associated Pulmonary Aspergillosis; EORTC-MSG: European Organization for Research and Treatment of Cancer Mycoses Study Grou; JBI: Joanna Briggs Institute BAL: Broncho Alveolar Lavage; CIs: Confidence Intervals; SMD: Standardised Mean Differences; GRADE: Grading of Recommendations, Assessments, Developments and Evaluations.

With the increasing global burden of coronavirus disease 2019 (COVID-19) cases; there has been a concomitant rise in incidence of secondary bacterial and fungal co-infections [1]. Viral pneumonia, in general, is associated with an increased incidence of secondary co- infections, and this is estimated to be between 6%-16% in critically ill patients with COVID-19 [2]. COVID-19 associated pulmonary aspergillosis (CAPA) has being increasingly reported worldwide, which is associated with increased mortality and morbidity [3]. It has been postulated that these co-infections are secondary to dysregulated immune responses associated with COVID-19 itself or due to the use of adjunctive therapies such as corticosteroids or interleukin-6 (IL-6) antagonists [2,4,5,6]. Prior reviews reported that the CAPA incidence varies between 10-13% [6-8,9]. However, the true incidence of CAPA in critically ill hospitalized patients is still undetermined due to diagnostic challenges involved as well as the observational nature of the published studies. With new studies being published, we conducted this systematic review and meta-analysis to explore the incidence, risk factors and outcomes associated with invasive pulmonary aspergillosis (IPA) in critically ill patients with COVID-19 [4,6,10].

Search strategy and selection criteria

This review was registered with PROSPERO (CRD42021227821) and was conducted in adherence with the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) statement. We searched Medline, Embase, Cochrane, Scopus, medRxiv databases from 1st December 2019 through 31st December 2021 using the following keywords and their variations: “COVID-19” and “aspergillosis” (Supplementary Table 1) [11]. We assessed all the relevant studies, and their citation lists to identify articles for inclusion. All studies reporting on at least 10 critically ill adult patients (≥ 18 years) with COVID-19 were included. We excluded any non-human studies, and any case reports to avoid publication bias. In the case of overlapping patient data across two or more studies, we included the larger study

Study	CAPA	Total	Incidence of CAPA (%)	Incidence (%)	95% CI	Weight
Autier 2021	67	239		28.0	[22.4; 34.2]	2.0%
Bartoletti 2020	30	185		16.2	[11.2; 22.3]	2.0%
Borman 2020	15	719		2.1	[ 1.2; 3.4]	2.0%
Boyd 2021	0	55		0.0	[ 0.0; 6.5]	1.9%
Bretange 2021	154	244		63.1	[56.7; 69.2]	2.0%
Chauvet 2020	6	46		13.0	[ 4.9; 26.3]	1.8%
Delliere 2020	21	366		5.7	[ 3.6; 8.6]	2.0%
Dupont 2020	19	106		17.9	[11.2; 26.6]	1.9%
Ergun 2021	58	219		26.5	[20.8; 32.9]	2.0%
Fekkar 2021	7	145		4.8	[ 2.0; 9.7]	1.9%
Ghazanfari 2021	22	105		21.0	[13.6; 30.0]	1.9%
Gregoire 2021	9	141		6.4	[ 3.0; 11.8]	1.9%
Hatzl 2021	10	132		7.6	[ 3.7; 13.5]	1.9%
Hoenigl 2021	28	59		47.5	[34.3; 60.9]	1.9%
Iqbal 2021	61	307		19.9	[15.6; 24.8]	2.0%
Janssen 2021 cohort 1	42	519		8.1	[ 5.9; 10.8]	2.0%
Janssen 2021 cohort 2	21	304		6.9	[ 4.3; 10.4]	2.0%
Jasim 2021	11	102		10.8	[ 5.5; 18.5]	1.9%
Kluzik 2021	7	19		36.8	[16.3; 61.6]	1.6%
Koehler 2020	5	19		26.3	[ 9.1; 51.2]	1.6%
Lahmer 2021	11	32		34.4	[18.6; 53.2]	1.8%
Lamoth 2020	3	118		2.5	[ 0.5; 7.3]	1.9%
Machado 2020	8	239		3.3	[ 1.5; 6.5]	2.0%
Maes 2021	3	81		3.7	[ 0.8; 10.4]	1.9%
Martin 2021	3	19		15.8	[ 3.4; 39.6]	1.6%
Meijer 2021	13	66		19.7	[10.9; 31.3]	1.9%
Nasir 2020	5	23		21.7	[ 7.5; 43.7]	1.7%
Nebreda−Mayoral 2021	3	113		2.7	[ 0.6; 7.6]	1.9%
Oliva 2021	0	55		0.0	[ 0.0; 6.5]	1.9%
Paramythiotou 2021	6	179		3.4	[ 1.2; 7.2]	2.0%
Prattes 2021	109	592		18.4	[15.4; 21.8]	2.0%
Rabagliati 2021	13	146		8.9	[ 4.8; 14.7]	1.9%
Ranhel 2021	10	248		4.0	[ 2.0; 7.3]	2.0%
Razazi 2020	13	90		14.4	[ 7.9; 23.4]	1.9%
Ripa 2020	11	731		1.5	[ 0.8; 2.7]	2.0%
Roman-Montes 2020	14	144		9.7	[ 5.4; 15.8]	1.9%
Rutsaert 2020	4	34		11.8	[ 3.3; 27.5]	1.8%
Segrelles-Calvo 2020	7	215		3.3	[ 1.3; 6.6]	2.0%
Sivasubramanian 2021	48	970		4.9	[ 3.7; 6.5]	2.0%
Sogaard 2021	2	41		4.9	[ 0.6; 16.5]	1.8%
Szabo 2021	20	20		100.0	[83.2; 100.0]	1.7%
Takazono 2021	10	10		100.0	[69.2; 100.0]	1.4%
Tio 2021	4	50		8.0	[ 2.2; 19.2]	1.8%
van Arkel 2020	6	31		19.4	[ 7.5; 37.5]	1.8%
van Grootveld 2021	11	63		17.5	[ 9.1; 29.1]	1.9%
Velez 2021	16	83		19.3	[11.4; 29.4]	1.9%
Versyck 2021	2	54		3.7	[ 0.5; 12.7]	1.9%
Wang 2020	0	26		0.0	[ 0.0; 13.2]	1.7%
Wasylyshyn 2021	3	256		1.2	[ 0.2; 3.4]	2.0%
White 2021	25	135		18.5	[12.4; 26.1]	1.9%
Xu 2021	78	393		19.8	[16.0; 24.1]	2.0%
Yusuf 2021	10	92		10.9	[ 5.3; 19.1]	1.9%
Zhang 2021	33	1633		2.0	[ 1.4; 2.8]	2.0%
Random effects model Heterogeneity: I2= 96.3%		11013		13.0	[8.7; 18.0]	100.0%

Table 1: Pooled incidence of COVID-19 associated pulmonary aspergillosis among critically ill patients with COVID-19.

Data collection

Data were collected using a prespecified data extraction form, and covered study characteristics (study design, study duration, name and country of study centre), patient demographics (sample size, number of male/female patients, age, comorbidities), Intensive Care Unit (ICU) characteristics (time to CAPA from onset of COVID-19 symptoms, classification system for CAPA, methods used to diagnose CAPA (bronchoscopic and non-bronchoscopic techniques), PaO2/FiO2 ratio, use of IL-6 antagonists and corticosteroids), patient outcomes (incidence of proven, probable, putative, and possible CAPA, incidence of Aspergillus colonisation, CAPA-associated mortality) and other relevant clinical outcomes (ICU length of stay [LOS] and duration of Invasive Mechanical Ventilation [IMV]).

CAPA is defined as IPA in temporal proximity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in patients requiring ICU admission due to respiratory failure. We defined proven, probable, putative and possible CAPA for this review as per the: Influenza-Associated Pulmonary Aspergillosis (IAPA) case definition, 2) the European Organization for Research and Treatment of Cancer Mycoses Study Group (EORTC-MSG), 3) crude or modified Aspergillosis in ICU (crude/mAsp-ICU) criteria or 4) 2020 European Confederation for Medical Mycology and the International Society for Human and Animal Mycology (ECMM/ISHAM) consensus criteria.2,12-14 In cases where both the crude Asp-ICU and mAsp-ICU criteria were used, we chose the mAsp-ICU criteria to define CAPA [2,12-14].

Risk of bias assessment

We used the appropriate Joanna Briggs Institute (JBI) critical appraisal checklists (Supplementary Table 2) to assess the eligibility of studies. The possibility of publication bias was assessed using Egger’s test. Two sensitivity analyses were performed for our meta-analysis: One where we excluded studies which had comparatively higher risks of bias (JBI score<8). The screening of articles, data collection, and risk of bias assessment were conducted independently by at least two reviewers (RRL, SAM, MRL, and SM), any conflicts were resolved by KR.

Meta-analysis	Number of studies	Incidence of CAPA (%)	CAPA	95%-CI
Colonisation Heterogeneity: I2 =89%, τ2 =0.0158, p<0.01	11		3.9	[1.2; 7.8]
Possible Heterogeneity: I2 =88%, τ2 =0.0061, p<0.01	16		2.3	[1.1; 3.8]
Probable Heterogeneity: I2 =97%,τ2 =0.0376, p<0.01	29		8.6	[4.9; 13.2]
Putative Heterogeneity: I2 =91%, τ2 =0.0506, p<0.01	18		9.3	[3.7; 16.8]
Proven Heterogeneity: I2 =91%, τ2 =0.0188, p<0.01	11		2.4	[0.3; 6.0]

Table 2: Pooled incidence of COVID-19 associated pulmonary aspergillosis among critically ill patients with COVID-19 stratified by definition.

Statistical analysis

Statistical analyses were performed on R4.0.2. For continuous variables, we pooled the means and standard deviations from the aggregate data presented in each study as per Wan, et al. [15] The primary outcome was the overall incidence of CAPA. Secondary outcomes included CAPA-associated mortality, ICU LOS, duration of IMV, and the time between the onset of COVID-19 symptoms and diagnosis of CAPA. We anticipated significant inter-study heterogeneity given variations in the demographics of patients with CAPA and its subsequent management in different countries. As such, random-effects meta-analyses (DerSimonian and Laird) were conducted, and 95% confidence intervals (CIs) were computed using the Clopper-Pearson method. Survival outcomes are presented as pooled proportions, dichotomous outcomes as pooled risk ratios (RR), and continuous outcomes as pooled means or mean differences (MD), each with their respective 95%-CIs [16,17]. Planned subgroup analyses were conducted with continuity correction to include studies with zero events, and included: The definition of CAPA (proven, probable, putative, and possible), study type (cohort studies, case control studies, case series), geographical region (Europe, Asia-Pacific, South America, North America, or International), the consensus definitions that were used in each study (EORTC-MSG, Asp-ICU [crude and/or modified], IAPA, 2020 ECMM/ISHAM, or mixed), and the methods of diagnosis {bronchoalveolar lavage (BAL), or no BAL}. Post-hoc subgroup analyses include timing of patient enrolment (before and after the publication of the Randomised Evaluation of COVID-19 Therapy (RECOVERY) trial final report in February 2021. Univariable study-level meta-regression was conducted when at least 6 data points were collected to explore potential sources of heterogeneity or prognostically-relevant study-level covariates [18]. As inter-study heterogeneity can be misleadingly large when assessed using I2 statistics for observational studies, we used the Grading of Recommendations [19,20], Assessments, Developments and Evaluations (GRADE) approach to assess the inter-study heterogeneity [21,22].

Of the 832 references screened; our search yielded 127 potentially relevant studies across the four databases (Supplementary Figure 1: PRISMA chart). 53 retrospective observational studies reporting on 11,013 adult patients with COVID-19 admitted to the ICU were included [23-74]. There were 24 cohort studies, 2 case control studies and 24 case series; 38 studies were from Europe, 7 from Asia, 5 from North America, 1 from South America, and 2 were conducted internationally. 44 studies reported the criteria that they used to diagnose CAPA: 7 studies diagnosed patients with CAPA using the EORTC-MSG criteria, 8 studies used either the crude Asp-ICU or mAsp-ICU criteria, 3 study used the IAPA case definition, 16 studies used the ECMM/ISHAM criteria, and 9 studies reported CAPA using two or more of the above criteria. All studies except for 6 employed BAL to diagnose CAPA. Only one study employed histopathological examination to diagnose CAPA.

Baseline demographics

The pooled age of patients with COVID-19 patients in the ICU was 62.5 years (95%-CI: 60.8-64.3). They were predominantly male (63.2% (95%-CI: 56.0-70.1%, 30 studies) with moderate-to-severe ARDS (PaO2/FiO2 ratio: 130.9, 95%-CI: 86.1-175.7, 8 studies). Patients with CAPA were older (+3.1 years, 95%-CI: 1.3-4.9, p=0.0006, 14 studies) and predominantly comprising males (RR: 1.14, 95%-CI: 1.0- 1.21, p<0.0001, 14 studies) when compared to COVID-19 patients without CAPA. The pooled prevalence of hypertension (HTN, 30 studies), obesity (17 studies), diabetes mellitus (DM, 39 studies) and chronic obstructive pulmonary disease (COPD, 15 studies) were 27.2% (95%-CI: 17.2%-38.5%), 19.1% (95%-CI: 9.6%-30.7%), 18.4% (95%- CI: 13.8%-23.4%) and 9.7% (95%-CI: 4.8%-16.1%) respectively. The prevalence of IL-6 antagonists and corticosteroid therapy were 8.2% (95%-CI: 3.6%-14.3%, 21 studies) and 26.3% (95%-CI: 15.7%-38.4%, 29 studies) respectively. All the included patients were admitted in intensive care unit (ICU).

Primary outcomes

Of 53 observational studies (11,013 critically ill patients with COVID-19), 1097 patients had CAPA; the pooled overall CAPA incidence was 13.0% (95%-CI: 8.7%-18.0%, moderate certainty, Table 1), with significant publication bias (p_egger=0.002, Supplementary Figure 2). After excluding studies with a JBI score of <8, the pooled overall incidence of CAPA was 12.7% (95%-CI: 8.0% to 18.3%). The incidence of CAPA changed significantly {4.1% (95%-CI: 1.1% to 8.4%)} after correcting for small study effects using the random-effects (R0 estimator) trim-and-fill procedure.

Subgroup analysis

The pooled incidence of colonisers (11 studies), possible (16 studies), probable (29 studies), putative (18 studies) and proven CAPA (11 studies), was 3.9% (95%-CI: 1.2%-7.8%), 2.3% (95%-CI: 1.1%- 3.8%),8.6% (95%-CI: 4.9%-13.2%), 9.3% (95%-CI: 3.7%-16.8%) and 2.4% (95%-CI: 0.3%-6.0%) respectively (Table 2). The pooled incidence of CAPA among studies from Europe (38 studies), Asia (7 studies), North America (5 studies), International (2 studies) and South America (1 study) was 12.2% (95%-CI: 7.5%-17.9%), 22.0% (95%-CI: 3.0%- 50.2%), 5.8% (95%-CI:1.4%-12.6%), 31.4% (95%-CI:7.6%-62.1%) and 8.9% (95%-CI:4.8% to 14.1%) respectively. The CAPA incidence based on ECMM/ISHAM (16 studies), Asp-ICU (8 studies), EORTC-MSG (7 studies), IAPA (3 studies) and mixed (9 studies) consensus criteria was 12.2% (95%-CI: 8.3%-16.8%), 9.1% (95%-CI:2.4%-18.9%), 7.9% (95%-CI:4.3% to 12.4%), 6.8% (95%-CI: 0.9%-16.8%) and 19.6% (95%- CI: 4.3%-41.8%) respectively found no significant difference (p=0.16). CAPA incidence was estimated to be 15.5% (95%-CI:9.5%-22.5%) when BAL was used for diagnosis compared to 9.9% (95%-CI:4.4%-17.1%) when non-bronchoscopic techniques were advocated for diagnosis (p>0.05). No significant difference ( p=0.44) in CAPA incidence was noted between pre-RECOVERY (43 studies, 14.1%, 95%-CI: 8.8-20.3%) and post RECOVERY trials (9 studies, 10.7%, 95%-CI: 5.1%-17.8%). There was no significant difference in the pooled incidence reported between study types (p=0.81). The details of the subgroup analysis are summarised in Table 3.

Table 3: Pooled incidence of COVID-19 associated pulmonary aspergillosis among critically ill patients with COVID-19.

Meta-regression analyses

Univariable meta-regression found that the prevalence of HTN (Regression co-efficient [B]: 0.559, 95%-CI: 0.212-0.905, p=0.002, Supplementary Figure 3) and corticosteroids (B:0.506, 95%-CI: 0.097-0.915, p=0.015, Supplementary Figure 4) use were significantly associated with increased CAPA incidence, while overall sample size was negatively associated with the incidence of CAPA (B:-0.002, 95%-CI:-0.005 to-0.000, p=0.037, Supplementary Figure 5). Other demographic factors such as age, prevalence of male patients, use of IL-6 antagonists and other comorbidities were not associated with the incidence of CAPA. The details of the meta-regression analyses are summarised in Table 4.The availability of simplified analytic modeling tools that can help decision makers determines when and how to reopen certain congregate settings, like schools, is an absolute necessity. In this research, we offer a strategic analytic tool for utilization of low-cost antigen tests in a comprehensive, targeted testing strategy, which in our perspective as academics specializing in business and biotechnology management is critical and allows for effective use of the various planning and execution protocols. Furthermore, strategic deployments have the potential to improve dramatically the production, procurement, and distribution of test kits, and can be of critical help to control and mitigate the spread of the SARS-CoV-2 virus in the U.S., and around the globe.

Table 4: Pooled incidence of COVID-19 associated pulmonary aspergillosis among critically ill patients with COVID-19 stratified by definition.

Secondary outcomes

Overall CAPA-associated mortality (42 studies, 814 patients with CAPA) was 63.4% (95%-CI: 56.2%-70.4%, moderate certainty, Table 5). CAPA was associated with increased risk of mortality in critically ill patients (18 studies, RR: 2.13 (95%-CI: 1.80-2.52, p<0.0001) compared to critically ill patients without CAPA. The pooled mean time for diagnosis of CAPA (19 studies, 353 patients with CAPA) was made 12.8 days (95%-CI: 10.5-15.1, moderate certainty) after the onset of COVID-19 symptoms. The pooled ICU LOS among patients with CAPA (13 studies, 287 patients) was 18.4 days (95%-CI: 13.7-23.1, moderate certainty), but there was no significant mean difference (MD) in ICU LOS between patients with and without CAPA (8 studies, 0.22 days, 95%-CI:-4.23 to 4.68, p=0.92). The mean duration of IMV among patients with CAPA was 17.2 days (5 studies, 95%-CI:15.5-19.0, moderate certainty).

Study	Mortality	CAPA	Mortality (%)	Mortality (%)	95% CI	Weight
Maes 2021	1	3		33.3	[ 0.8; 90.6]	1.1%
Martin 2021	1	3		33.3	[ 0.8; 90.6]	1.1%
Lamoth 2020	1	3		33.3	[ 0.8; 90.6]	1.1%
Wasylyshyn 2021	1	3		33.3	[ 0.8; 90.6]	1.1%
Nebreda-Mayoral 2021	2	3		66.7	[ 9.4; 99.2]	1.1%
Versyck 2021	2	2		100.0	[15.8; 100.0]	0.9%
Koehler 2020	3	5		60.0	[14.7; 94.7]	1.6%
Ranhel 2021	3	10		30.0	[ 6.7; 65.2]	2.3%
Nasir 2020	3	5		60.0	[14.7; 94.7]	1.6%
Tio 2021	3	4		75.0	[19.4; 99.4]	1.4%
Lahmer 2021	4	11		36.4	[10.9; 69.2]	2.4%
Rutsaert 2020	4	4		100.0	[39.8; 100.0]	1.4%
Paramythiotou 2021	4	6		66.7	[22.3; 95.7]	1.7%
Fekkar 2021	4	7		57.1	[18.4; 90.1]	1.9%
Chauvet 2020	4	6		66.7	[22.3; 95.7]	1.7%
Rabagliati 2021	4	13		30.8	[ 9.1; 61.4]	2.5%
van Arkel 2020	4	6		66.7	[22.3; 95.7]	1.7%
Gregoire 2021	5	9		55.6	[21.2; 86.3]	2.1%
Segrelles-Calvo 2020	5	7		71.4	[29.0; 96.3]	1.9%
Takazono 2021	5	10		50.0	[18.7; 81.3]	2.3%
Velez 2021	5	16		31.2	[11.0; 58.7]	2.7%
Meijer 2021	6	13		46.2	[19.2; 74.9]	2.5%
Kluzik 2021	7	7		100.0	[59.0; 100.0]	1.9%
Dupont 2020	7	19		36.8	[16.3; 61.6]	2.9%
Hatzl 2021	8	10		80.0	[44.4; 97.5]	2.3%
Machado 2020	8	8		100.0	[63.1; 100.0]	2.0%
Roman-Montes 2020	8	14		57.1	[28.9; 82.3]	2.6%
Janssen 2021 cohort 2	9	21		42.9	[21.8; 66.0]	3.0%
van Grootveld 2021	10	11		90.9	[58.7; 99.8]	2.4%
Szabo 2021	12	20		60.0	[36.1; 80.9]	3.0%
White 2021	13	25		52.0	[31.3; 72.2]	3.2%
Delliere 2020	15	21		71.4	[47.8; 88.7]	3.0%
Bartoletti 2020	16	30		53.3	[34.3; 71.7]	3.3%
Hoenigl 2021	18	28		64.3	[44.1; 81.4]	3.2%
Ghazanfari 2021	20	22		90.9	[70.8; 98.9]	3.0%
Janssen 2021 cohort 1	22	42		52.4	[36.4; 68.0]	3.5%
Zhang 2021	22	33		66.7	[48.2; 82.0]	3.4%
Ergun 2021	29	58		50.0	[36.6; 63.4]	3.7%
Sivasubramanian 2021	40	48		83.3	[69.8; 92.5]	3.6%
Xu 2021	51	78		65.4	[53.8; 75.8]	3.9%
Iqbal 2021	56	61		91.8	[81.9; 97.3]	3.8%
Prattes 2021	62	109		56.9	[47.0; 66.3]	4.0%
Random effects model Heterogeneity: I2 = 65.7%		814		63.4	[56.2; 70.4]	100.0%

Table 5: Pooled proportion of non-survivors among critically ill patients with COVID-19 associated pulmonary aspergillosis.

Assessment of study quality

Based on the JBI critical appraisal checklists for cohort studies, case control studies, and case series, the majority studies included for this review were of high quality according to the appropriate checklist (Supplementary Table 2). There was moderate certainty on the level of evidence for the primary outcome. A summary of the assessment of certainty using the GRADE approach is presented in Table 6.

Table 6: Pooled proportion of non-survivors among critically ill patients with COVID-19 associated pulmonary aspergillosis.

This review highlighted the incidence, characteristics and outcomes of critically ill patients with CAPA in the first two years of the COVID-19 pandemic. Around 13% of critically ill older and mostly male patients with COVID-19 in ICU developed CAPA, with a significant publication bias in the incidence of CAPA. Our meta- analysis found a high mortality rate (63.4%) in patients with CAPA. We noted that patients with hypertension and those received

corticosteroids were at higher risk of contracting CAPA. However, we failed to note any significant difference in CAPA incidence between pre-and post-RECOVERY trial.

Immune dysregulation is commonly observed in critically ill patients with COVID-19, predisposing them to potentially fatal invasive fungal infections. Also, COVID-19 results in impaired ciliary function and decreased lymphocytes count that predispose these patients to IPA [75]. We observed the pooled incidence of CAPA in our critically ill cohort was 13%. Similarly, Mitaka, et al. [6,76]. and Chong, et al. reported overall CAPA incidence of 10.2% and 13.5% respectively. Our analysis demonstrated that observational studies with a large sample size had a lower incidence of CAPA, thereby pointing towards reporting bias in studies with smaller sample size [6,9]. We noted that corticosteroids usage was significantly associated with an increased incidence of CAPA in ICU patients; this could be potentially attributable to their immunomodulatory properties which increase host susceptibility to invasive Aspergillus infection. Our subgroup analysis failed to demonstrate any such increase in CAPA incidence between pre-and post-RECOVERY trials. We were somewhat surprised that IL-6 antagonists were not found to be a risk factor for CAPA in this meta-analysis, but there were only 8% of patients in the published studies who were on IL-6 antagonists [19,20].

There are multiple challenges in diagnosing the true incidence of CAPA in critically ill patients. Rather than a standardised definition to classify CAPA, [2] various criteria like IAPA case definition, EORTC- MSG, crude/mAsp-ICU or ECMM/ISHAM consensus criteria were used to individually define CAPA. In addition to this, typical host factors or radiological features described in these classification systems might not apply to patients with CAPA [2,12-14]. However, while mycological evidence is pivotal in diagnosing CAPA, [2,10] it is hampered by the difficulties in distinguishing colonisation from angio-invasive disease [2]. Interestingly, oursubgroup analysis demonstrated that the various case definitions were not significantly different in estimating the CAPA incidence in this cohort [2]. Another reason for heterogeneity in estimating the incidence may be due to differences in CAPA screening in intensive care unit. Galactomannan testing from BAL fluid is the most sensitive test for diagnosing IPA in ICU patients; [77,78] however, BAL is infrequently carried out in critically ill patients with COVID-19 due to aerosol generation and risk of disease transmission. Up to 80% of positive respiratory samples without biopsies from critically ill immune competent hosts are colonised samples and not IPA, [79-82] it may be plausible that colonised samples were falsely reported as CAPA because consensus criteria was not clearly defined until recently. Along with the abovementioned points, using diagnostic bronchoscopy without employing histological or cytological examinations to diagnose CAPA routinely could potentially lead to over-diagnosis of CAPA among critically ill patients [2]. Our subgroup analysis failed to note any significant difference in estimating CAPA incidence based on various methods of diagnosis.

Well known studies on IPA and recent literature on CAPA both suggest that Aspergillus co-infection may contribute to increased mortality. High mortality rates (35% to 70%) have been reported among critically ill patients with IPA [2,6]. Prior reviews noted pooled mortality from CAPA was 48% to 55% [14,83]. In contrast to these findings, the pooled mortality among patients with CAPA in our review was 63.4% [6,9,84]. The increased mortality among patients with CAPA can potentially be explained by the severity of COVID-19. Previous reviews have shown that age is a risk factor for disease severity and mortality. In line with previous single-centre observational studies, our review found that patients with CAPA were older than patients without CAPA, and possibly experience more severe disease, leading to higher mortality rates [85]. From this perspective, we believe that there is reasonable justification to routinely screen critically ill patients with COVID-19 for CAPA if they remain without improvement, or rapidly deteriorate after initial improvement from COVID-19, and especially if the patients have received immunomodulatory treatments such as corticosteroids either alone or with IL-6 antagonists. Consideration can be given for clinical trials to determine whether antifungal prophylaxis early screening and preemptive treatment will safely reduce the incidence and overall mortality in critically ill COVID-19 patients.

The strengths of this review include robust inclusion and exclusion criteria. Our review included more than 50 studies encompassing 11,000 critically ill patients with COVID-19 across the globe. In contrast to the previous reviews’ which reported CAPA incidence in the general population, this is the first study to highlight incidence of CAPA in critically ill patients with COVID-19. We reduced confounding and accounted for heterogeneity by elucidating factors correlating with CAPA incidence via subgroup analysis and meta regression. Nonetheless, we recognize several limitations of this study. The significant publication bias, inverse relationship with sample size along and lack of granularity in diagnosis criteria make the true estimation of CAPA incidence difficult. This could also be attributed to the inability to collect respiratory specimens from all eligible patients in the context of overstretched resources due to the pandemic.

The results should be interpreted with caution as this could potentially point to a significant overestimation of CAPA among critically ill patients with COVID-19. Searches for unpublished manuscripts and pre-print texts to reduce publication bias did not yield any articles for inclusion. Data related to the duration of IMV was scarce, so it is difficult to assess whether this is also a risk factor for CAPA. Also, the patients were not stratified based on age, which could be a plausible risk factor for CAPA. Owing to the paucity of data, it was difficult to determine whether patients received corticosteroids specifically for COVID-19 or were on long-term therapy for any underlying illness. Finally, our analysis is based mainly on retrospective studies with significant heterogeneity, which can introduce confounding factors given the lack of risk-adjustment or propensity-score techniques. However, JBI critical appraisal of the included studies suggests that most of the articles are of high quality, and GRADE assessment suggested moderate certainty of the evidence in our review.

Clinicians should be cognizant that critically ill patients with COVID-19 may acquire CAPA, especially in those who are receiving corticosteroids. The outcomes for patients with CAPA are poor; an earlier diagnosis with multimodal diagnostic workup and management with pre-emptive antifungal agents should be considered on a case- by-case basis. With numerous diagnostic challenges involved, future studies should use a standardized definition to stratify patients at risk of or with CAPA, increase suspicion and early diagnosis of CAPA, and ideally

improve overall patient outcomes. This may be even more necessary in the post-RECOVERY trial era, where corticosteroids often with IL-6 inhibitors are being routinely used to treat hypoxaemic patients with COVID-19

None

None

All authors agreed for publication of this study

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

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